This company does not care about their workers. Some workers would work 16 hour days with barley 30 min break. They were not understanding at all. Many people only lasted a few weeks and then just left. The training was not organized once so over and the company runs on very old machinery. Cons training was not organized The company has a large business volume and stable income, but lacks incentives in management and provides professional development for employees. The boss is willing to listen to the opinions of the employees. He is a harmonious person. I hope they can improve the incentive mechanism and provide staff with professional development guidance. This company is a great place for new grads because they are willing to teach. Colleagues are nice and the manager has wide knowledge and experience. The salary is reasonable and with insurance benefits. Plus they have 401K and paid time vocation. Cons You might need to work overtime but with extra pay. Elim is a good place for the employee who really would like to develop their professional career.

Working at Elim Biopharmaceuticals Inc: Employee Reviews | Indeed.com

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These included: Electrolyte abnormalities (43%), such as hyperkalemia, hypokalemia, hyponatremia, or hypercalcemia Myelosuppression (35%), such as reductions in absolute neutrophil count, white blood cell counts, lymphopenia, hemoglobin, or hematocrit Increased liver enzymes, such as aspartate aminotransferase (35%), or alanine aminotransferase (27%) These laboratory abnormalities often improved while continuing ZOKINVY, but it is not possible to exclude ZOKINVY as a cause of the abnormalities. Periodically monitor electrolytes, complete blood counts, and liver enzymes, and manage abnormalities accordingly. Nephrotoxicity Lonafarnib caused nephrotoxicity in rats at plasma drug exposures approximately equal to that achieved with the human dose. Monitor renal function at regular intervals during ZOKINVY therapy. Retinal Toxicity Lonafarnib caused rod-dependent, low-light vision decline in monkeys at plasma drug exposures similar to that achieved with the human dose. Perform ophthalmological evaluation at regular intervals and at the onset of any new visual changes during ZOKINVY therapy.